3 5 Difluoroiodobenzene
Iodobenzene

3,5-Difluoroiodobenzene

Fengxi Chemical

    Specifications

    HS Code

    667827

    Chemical Formula C6H3F2I
    Molecular Weight 253.99
    Appearance Colorless to light yellow liquid
    Boiling Point 173 - 175 °C
    Melting Point N/A
    Density 1.984 g/mL at 25 °C
    Flash Point 66 °C
    Solubility Insoluble in water, soluble in organic solvents like ethanol, ether
    Vapor Pressure N/A
    Refractive Index 1.5720 - 1.5740

    As an accredited 3,5-Difluoroiodobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 500g of 3,5 - difluoroiodobenzene packaged in a sealed glass bottle.
    Storage 3,5 - difluoroiodobenzene should be stored in a cool, dry, well - ventilated area away from heat sources and ignition sources. It should be kept in a tightly sealed container to prevent leakage and exposure to air and moisture. Store it separately from oxidizing agents and incompatible substances to avoid potential chemical reactions.
    Shipping 3,5 - difluoroiodobenzene is shipped in well - sealed, corrosion - resistant containers. Shipment follows strict hazardous chemical regulations, ensuring proper handling, temperature control, and documentation for safe transport.
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    3,5-Difluoroiodobenzene
    General Information
    Historical Development
    3,5-Difluoroiodobenzene is also an organic compound. Its initial research began many years ago. At that time, the research of various scholars was to explore its characteristics and uses.
    At the beginning, the synthesis method was still simple, but the yield was not ideal. Scholars worked hard to improve the process. After many attempts, the new synthesis path gradually became clear, and the yield also increased significantly.
    The early application was rather narrow, only seen in a few experiments. After in-depth investigation, it emerged in the field of medicinal chemistry, and can be used as a key intermediate to help the development of new drugs.
    Its historical evolution is the result of the efforts of many chemists. Since the initial exploration, it has been widely used today, and every step has involved difficulties and breakthroughs, making it an indispensable part of chemical research.
    Product Overview
    Description of 3,5-Difluoroiodobenzene
    There is a product called 3,5-difluoroiodobenzene. It is an organic halide, which is of great value in the field of chemical and pharmaceutical synthesis.
    Looking at its shape, at room temperature, it is a colorless to light yellow transparent liquid with pure texture. Smell it, it has a slightly special smell. Its physical and chemical properties are unique, and the boiling point is within a certain range. At this temperature, the substance gradually changes from liquid to gaseous state, which is conducive to separation and purification.
    In terms of its use, it is a key intermediate in pharmaceutical research and development. By means of organic synthesis, a variety of complex molecular structures can be constructed, which can help the creation of new drugs. In chemical production, it is also an important raw material and participates in the preparation of many fine chemicals.
    In the process of preparation, through a specific chemical reaction, according to a precise process, the reactants are reacted under suitable conditions, and the pure product is obtained through multiple processes. However, when preparing, it is necessary to strictly follow the operating procedures to ensure safety and quality.
    In short, 3,5-difluoroiodobenzene plays an important role in today's chemical-related industries and has broad prospects. It needs to be further explored by researchers to develop its more potential.
    Physical & Chemical Properties
    3,5-Difluoroiodobenzene is also an organic compound. Its physical properties, at room temperature, are colorless to light yellow liquids with a special odor. Its boiling point is suitable for a certain range, and the density also has a specific value. In organic solvents, it exhibits good solubility.
    On chemical properties, the presence of fluorine atoms and iodine atoms in this compound gives it unique reactivity. Fluorine atoms have strong electronegativity, which changes the density distribution of electron clouds in the benzene ring, affecting the check point and activity of electrophilic substitution reactions. Iodine atoms are relatively active and can participate in a variety of nucleophilic substitution reactions. They can interact with many nucleophilic reagents to achieve the transformation of functional groups. In the field of organic synthesis, they are often important intermediates for building complex molecular structures. Due to their special physical and chemical properties, they play a role in the stage of organic chemical synthesis.
    Technical Specifications & Labeling
    "3,5-Difluoroiodobenzene Technical Specifications and Labeling (Commodity Parameters) "
    There are 3,5-difluoroiodobenzene today, and its technical specifications are related to the preparation method. It needs to be in a suitable reaction vessel and controlled to precise temperature and pressure. The ratio of raw materials must be accurate, such as [specific raw material 1] and [specific raw material 2] mixed in [X] ratio, and the specific reaction time can be used to make this good product.
    In terms of identification, the product parameters should be detailed. The appearance should be [specific appearance description], the purity should not be less than [X]%, and the impurity content must be strictly controlled. On the packaging, key information such as product name, content, and production date should be clearly marked to prevent confusion and misuse, and to ensure that this product can be safely and accurately applied in the chemical industry.
    Preparation Method
    This product of 3,5-Difluoroiodobenzene, raw materials and production process, reaction steps and catalytic mechanism are the key.
    First take fluorobenzene as the raw material, add a brominating agent, control the temperature to a moderate, and react with electrophilic substitution to obtain 3,5-dibromofluorobenzene. In this step, attention should be paid to the rate of the reaction and the purity of the product.
    Second, magnesium chips and anhydrous ether are used to make Grignard's reagent. Slowly inject 3,5-dibromofluorobenzene and stir to obtain 3,5-dibromophenyl magnesium reagent. This environment must be anhydrous and oxygen-free to prevent side reactions. After
    , take the iodine reagent and add it to the Grignard reagent prepared above. After the halogen exchange reaction, 3,5-Difluoroiodobenzene can be obtained. After the reaction is completed, the product can be purified by extraction, distillation and other methods.
    In this process, the catalyst can promote the speed of the reaction and the rate of product extraction. It is necessary to select the appropriate catalyst and control its dosage for the preparation of this product. In this way, according to this process, the product of 3,5-Difluoroiodobenzene can be obtained.
    Chemical Reactions & Modifications
    Nowadays, there is a chemical substance called 3,5-difluoroiodobenzene. In the field of chemical synthesis, its reaction and modification are extremely critical. To make this compound, a nucleophilic substitution method is often used, a suitable halogenated aromatic hydrocarbon is selected, and a fluorine source is added. Under specific temperature, pressure and catalyst, the fluorine atom is added to the benzene ring to form a 3,5-difluorine structure.
    As for its modification, or the introduction of other functional groups to change its physicochemical properties. It can be used by coupling reactions to connect different groups to expand its application. If it is coupled with an alkenyl-containing reagent to obtain a conjugated structure, it will increase its optoelectronic properties, which may be useful in the genus of optoelectronic materials.
    Or according to specific needs, adjust the reaction conditions, optimize the reaction path, reduce side reactions, and increase the purity and yield of the product. This is where chemical researchers focus on the reaction and modification of 3,5-difluoroiodobenzene.
    Synonyms & Product Names
    Hearing the Karma of Chemistry, 3,5 - Difluoroiodobenzene This thing is very important in our research. Its synonymous names also need to be explored in detail.
    Looking at the past, the names of chemical things often have similarities and differences due to regions and current situations. This 3,5 - Difluoroiodobenzene, or another name, but they all refer to the same thing.
    When we studied it, we knew the name of the synonym well, just like the help of a boat. Knowing its different titles, we can learn from people's opinions and widely accept the theories of various families. Or in ancient books, or in Western books, although the names are different, the actual meanings are the same.
    And the name of this thing in the business trip of the husband also needs to be clearly distinguished. Merchants use names to show things, and they are precise and correct, so that they can trade smoothly. Therefore, synonymous names and commodity names are all under the scrutiny of our chemical researchers. I hope to be able to know their details in detail, and it is beneficial to learn and do business, so as to help the prosperity of this industry.
    Safety & Operational Standards
    "Specifications for the Safety and Operation of 3,5-Difluoroiodobenzene"
    The use of 3,5-difluoroiodobenzene is also a chemical product. Its unique nature is related to experimental safety and operation regulations, which cannot be ignored.
    For storage, choose a cool, dry and well-ventilated place. Keep away from fire and heat sources to prevent accidents. Cover it or it may be flammable and explosive. If you are not careful, it will cause a disaster. Store it in a preservative and leak-proof device to avoid leakage and endanger the surroundings.
    As for the operation, be careful. The operator must wear appropriate protective equipment, such as protective clothing, gloves, goggles, etc., to guard against possible hazards. The operation room should also be well ventilated, and a complete ventilation system should be set up to allow harmful gases to escape in time and not stay.
    When taking it, the action should be slow, and it should be scooped slowly. Do not spill it. If there is any accidental spill, immediately dispose of it according to the established method. For small amounts, you can cover it with inert substances such as sand and vermiculite, collect it and dispose of it properly; for large amounts, quickly start an emergency case, evacuate everyone, and invite professional people to deal with it.
    Furthermore, for experimental equipment, use Bibijie to prevent the residual objects from reacting with other objects and causing harm. And in the entire operation process, it should be recorded in detail for future inspection, and there are traces to follow.
    In short, the safety and operation specifications of 3,5-difluoroiodobenzene are essential for the smooth experiment and the safety of personnel. It must not be taken lightly. It must be strictly followed to ensure safety.
    Application Area
    3,5-Difluoroiodobenzene is also a genus of chemical materials. Its application field is quite promising. In the field of medicinal chemistry, it can be used as a key intermediate. Because of its unique structure, it can make the synthesized drug molecules have specific activities and properties, or increase drug efficacy, or change pharmacokinetic characteristics, which is the cornerstone of the creation of new pharmaceuticals.
    In materials science, it is also useful. Can participate in the preparation of materials with special photoelectric properties. Such materials are used in optoelectronic devices, such as organic Light Emitting Diodes, solar cells, etc., or can improve the performance of devices, improve their luminous efficiency, stability, etc.
    In the field of fine chemicals, it is an important raw material for the synthesis of high-end fine chemicals. Through exquisite chemical reactions, a variety of products with unique functions can be derived to meet the needs of different industries and scientific research. Its wide application is waiting for our generation to explore in depth, so as to make the best use of it and promote the progress of chemistry and related fields.
    Research & Development
    Today, there is a product called 3,5-difluoroiodobenzene, which is of great significance in our chemical research. We have tried our best to study its characteristics. After long-term exploration, we found that the synthesis method requires delicate control of reaction conditions, such as temperature and the proportion of reagents. If there is a slight difference, it will be a thousand miles away.
    Its application is also wide, and it can be used as a key intermediate in the field of pharmaceutical creation to assist in the development of new drugs. It is expected to solve many diseases. In the field of materials science, it also has its unique capabilities, which may optimize material properties and open up new frontiers.
    However, we are well aware that the road to research is long and there are still many problems to be solved. Synthetic efficiency still needs to be improved, and costs need to be reduced. In the future, we should persevere and improve our skills, hoping to promote the development of this material and contribute to the progress of chemistry and the well-being of mankind.
    Toxicity Research
    I tried to study poisons, recently in 3,5 - Difluoroiodobenzene this substance has been a lot of effort. This substance also, the study of its toxicity, should not be ignored.
    Look at its properties, unique structure, fluorine and iodine, fluorine activity, iodine characteristics, the two are combined in the benzene ring, or toxic abnormalities. During the experiment, observe its impact on microorganisms, cells encounter, morphology, metabolism are changed, growth is blocked, and vitality gradually fades.
    However, the study of toxicity is not only microscopic. Consider its diffusion in the environment, if it escapes, enters the water and soil, and circulates in the biological chain, causing harm to all living beings. Therefore, the toxicity of 3,5 - Difluoroiodobenzene is related to life and the environment, and it must be carefully investigated to avoid future problems.
    Future Prospects
    I have tried to study chemical substances, and now I look at 3,5-difluoroiodobenzene, thinking about its future development, and I have expectations. This material is unique, and it may open up new paths in the field of organic synthesis.
    In the future, it may be able to emerge in the creation of medicine. Because of its special structure, it may be able to assist in the research of new drugs, cure various diseases, and seek well-being for the world. And in the field of materials science, it is also expected to become the foundation of new materials, giving unique properties to be used in high-tech and promoting its leap.
    Furthermore, the synthesis method can be improved. Researchers should find better paths, reduce costs and improve efficiency, so that this product can be widely used. At that time, 3,5-difluoroiodobenzene will shine in many fields, open up infinite possibilities for the future, open a new chapter of scientific and technological progress, and promote the grand cause of human development.
    Where to Buy 3,5-Difluoroiodobenzene in China?
    As a trusted 3,5-Difluoroiodobenzene manufacturer, we deliver: Factory-Direct Value: Competitive pricing with no middleman markups, tailored for bulk orders and project-scale requirements. Technical Excellence: Precision-engineered solutions backed by R&D expertise, from formulation to end-to-end delivery. Whether you need industrial-grade quantities or specialized customizations, our team ensures reliability at every stage—from initial specification to post-delivery support.
    Frequently Asked Questions

    As a leading 3,5-Difluoroiodobenzene supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    What are the main uses of 3,5-difluoroiodobenzene?
    3,5-Diethoxybenzoic acid is a key raw material and intermediate in organic synthesis, and is widely used in many fields. Its main uses are described below:
    ** 1. Drug synthesis field **
    In the field of pharmaceutical chemistry, it can be used as an important structural unit. Because this compound has a specific chemical structure and activity, it can participate in the construction process of various drug molecules. For example, it can be connected to a molecular framework with biological activity through a series of chemical reactions, so as to obtain drugs with specific pharmacological activities. In some synthetic routes of antibacterial and anti-inflammatory drugs, 3,5-diethoxybenzoic acid acts as a key starting material. With the functional groups such as ethoxy and carboxyl in its structure, it can react with other compounds such as esterification and amidation, and gradually build complex and specific drug molecular structures to achieve the purpose of treating related diseases.
    ** Second, the field of materials science **
    1. ** Modification of polymer materials **: In the preparation of polymer materials, 3,5-diethoxy benzoic acid can be added as a modifier. The functional groups it contains can chemically react with polymer chains, or interact with polymers by means of intermolecular forces, thereby changing the properties of polymer materials. For example, it can improve the thermal stability of polymer materials, so that the materials can still maintain good physical properties at higher temperatures, so as not to soften and deform prematurely. It can also enhance the solubility and processing properties of polymer materials, which is convenient for materials to be molded, such as injection molding, extrusion and other process operations.
    2. ** Preparation of functional materials **: Can be used to synthesize materials with specific functions. Taking optical materials as an example, by chemically modifying and assembling 3,5-diethoxybenzoic acid, materials with specific optical properties can be prepared, such as fluorescent materials. These materials show potential application value in the fields of optical sensing and display technology. They can be used to manufacture sensor devices, perform high-sensitivity optical detection of specific substances, or be applied to new display materials to improve display effects.
    ** III. Use of organic synthesis intermediates **
    1. ** Derivative other compounds **: Because the carboxyl group and ethoxy group in its structure have high reactivity, it can be converted into other functional groups through a variety of chemical reactions. For example, carboxyl groups can be converted into ester groups by esterification reaction, and a series of ester compounds with different structures and properties can be generated by reacting with different alcohols. These ester compounds have important uses in the fields of fragrances, coatings, etc. Some esters can be used as fragrance ingredients to give products unique aroma; in coatings, it can improve the film-forming performance and adhesion properties of coatings.
    2. ** Construction of complex organic molecules **: As a key intermediate in organic synthesis, it can participate in multi-step organic synthesis reactions to gradually build complex organic molecular structures. In the field of total synthesis of natural products, it is often used as one of the starting materials. By ingeniously designing the reaction route and reacting with other organic reagents, a carbon skeleton and functional group structure similar to that of natural products are gradually established, thus realizing the artificial synthesis of natural products and providing a material basis for the development of new drugs and biological activity research.
    What are the synthesis methods of 3,5-difluoroiodobenzene?
    There are several common methods for the synthesis of 3,2,5-diethoxybenzaldehyde:
    One is the synthesis path using resorcinol as the starting material. The resorcinol is first etherified with chloroethane in an alkaline environment, catalyzed by a suitable catalyst, to generate m-diethoxybenzene. Subsequently, the m-diethoxybenzene and the corresponding formylation reagent, such as in the presence of anhydrous zinc chloride and other catalysts, react with hydrogen cyanide and hydrogen chloride mixed gas, and obtain 3,2,5-diethoxybenzaldehyde after hydrolysis. In this process, the etherification reaction needs to pay attention to the control of the reaction temperature and the amount of base to avoid overreaction; the formylation step needs to pay attention to the precise control of the reaction conditions to ensure that the reaction proceeds in the direction of generating the target product.
    The second is to use benzaldehyde derivatives as starting materials. Select suitable benzaldehyde derivatives, and the substituents on them are gradually introduced into ethoxy groups under specific reaction conditions. For example, a halogen atom is first introduced into the benzaldehyde ring by a specific method, and then nucleophilic substitution reactions occur with reagents such as sodium ethanol, thereby introducing ethoxy groups. This process requires careful consideration of the order and conditions of each step of the reaction to ensure that the substituents are introduced in the expected position and quantity, and attention should be paid to the protection and de-protection of the aldehyde group during the reaction to avoid damage to the aldehyde group during the reaction or unnecessary reactions.
    Third, the phenolic compound through the Fu-g reaction can be considered as the initial step. Under the action of Lewis acid catalyst, the phenolic compound and halogenated ethane first form an ether structure, and then the aldehyde group is constructed through the subsequent formylation reaction. The activity and selectivity of the catalyst should be taken into account in the Foucault reaction. During formylation, the reaction parameters should be precisely adjusted according to the specific reagents and reaction systems used, so that the reaction can efficiently generate 3,2,5-diethoxybenzaldehyde.
    Each synthesis method has its own advantages and disadvantages. In practical applications, many factors such as the availability of raw materials, cost, difficulty in controlling reaction conditions, and purity of the product should be comprehensively considered, and the most suitable one should be selected for synthesis.
    What are the physical properties of 3,5-difluoroiodobenzene?
    3% 2C5-diethylthiophene is an organic compound with unique physical properties, detailed as follows:
    1. ** Properties **: Under normal conditions, 3% 2C5-diethylthiophene is mostly a colorless to light yellow transparent liquid. It is clear and pure in appearance and has no visible impurities to the naked eye. This property makes it easy to handle and operate in various chemical reactions and industrial applications.
    2. ** Odor **: It has a special aromatic smell, but its taste is more unique than common aromatic hydrocarbons, and it is difficult for non-professionals to describe it accurately. This smell can be used as a basis for identifying the substance to a certain extent.
    3. ** Boiling Point **: The boiling point is about 190-195 ° C. This boiling point characteristic determines its condition requirements in chemical operations such as distillation and separation. At a specific temperature, 3% 2C5-diethylthiophene can be converted from liquid to gaseous state, so as to separate from other substances with large differences in boiling points, and realize the purpose of purification or mixing.
    4. ** Melting point **: The melting point is low, about -50 ° C. The low melting point makes the substance stable in liquid state at room temperature, and it is not easy to solidify under cold conditions, ensuring its fluidity and reactivity at different ambient temperatures.
    5. ** Solubility **: It is difficult to dissolve in water, but can be miscible with most organic solvents such as ethanol, ether, benzene, etc. in any ratio. This solubility characteristic is related to its molecular structure, making it widely used in the field of organic synthesis. In the preparation of certain organic compounds, its miscibility with organic solvents can be used to construct a homogeneous reaction system and promote the reaction.
    6. ** Density **: The density is slightly larger than that of water, about 0.99 - 1.01 g/cm ³. This allows 3% 2C5-diethylthiophene and water to be stratified due to density differences, which is convenient for separation by means of liquid separation.
    What are the precautions for storing and transporting 3,5-difluoroiodobenzene?
    For 3% 2C5-diethylhydroquinone, many things should be paid attention to during storage and transportation.
    First storage method. This substance should be stored in a cool, dry and well-ventilated place. Due to its nature, if it is heated or damp, it may cause quality changes. The temperature of the warehouse should not be too high, and it should be maintained within a specific range as much as possible to prevent it from decomposing and other adverse conditions due to temperature. At the same time, it is necessary to keep away from fire and heat sources, and the threat of open flames cannot be ignored. This is the key to avoiding fires and explosions. Furthermore, it should be stored separately from oxidants and acids, and must not be mixed. Because different chemical substances may occasionally react violently, once the reaction is out of control, the consequences are unimaginable.
    As for transportation, there are also many precautions. Before transportation, it is necessary to ensure that the packaging is complete and sealed, which is the first step to prevent its leakage. During transportation, it is necessary to ensure that the container does not leak, collapse, fall or damage. Transportation vehicles should be equipped with corresponding varieties and quantities of fire-fighting equipment and leakage emergency treatment equipment for emergencies. If a leak occurs during transportation, do not panic. Immediate and effective measures should be taken to evacuate the surrounding personnel and prevent the occurrence of poisoning and other hazards. And when transporting, drive according to the specified route and do not stop in densely populated areas and residential areas to avoid large-scale harm caused by leakage. At the same time, transportation personnel also need to undergo professional training to be familiar with its characteristics and emergency treatment methods, so as to ensure maximum safety and avoid accidents when storing and transporting 3% 2C5-diethylhydroquinone.
    What is the market price of 3,5-difluoroiodobenzene?
    In today's world, business conditions are treacherous, and the price of the market is often changed due to various reasons. Ruofu 3,5-diethoxybenzoic acid, the price of its market is also not constant.
    For the first time, the supply and demand of raw materials are largely determined by their price. If the raw materials are abundant and the demand is small, the price is low; conversely, if the raw materials are rare and the demand is large, the price will be high. For example, the various herbs and minerals on which you depend, the habitat changes, and the harvest is different, can all make the price of 3,5-diethoxybenzoic acid different.
    Second, the simplicity and novelty of the process also affect its price. In the ancient method of processing, if the process is complicated and the manpower and material resources are expended a lot, the price will be high; if the new technique is skillfully developed, the cost will be reduced, and the price may be reduced. However, the creation of new techniques also requires capital investment. When it is first implemented, the price may increase due to the cost of research and development.
    Furthermore, the needs of the city are the key to the price. Such as in the field of medicine, if a party needs 3,5-diethoxybenzoic acid very urgently, the price will soar; if there is no big need and the goods are in stock, the price will slow down.
    There are also government decrees, and changes in taxes can also disturb its price. If the tax is heavy, the business will increase the price to protect its profits; if the government promotes its production, the price may be adjusted accordingly.
    In summary, the market price of 3,5-diethoxybenzoic acid is like Piaoping, which moves with the winds of raw materials, processes, requirements, and decrees. If you want to know its exact price, you can only judge the situation and observe the market situation carefully.